Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0005886 | plasma membrane | 3 | 1 |
Related structures:
AlphaFold database: A4H7L2
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006811 | monoatomic ion transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005215 | transporter activity | 1 | 11 |
GO:0005216 | monoatomic ion channel activity | 4 | 11 |
GO:0005227 | calcium activated cation channel activity | 6 | 11 |
GO:0005261 | monoatomic cation channel activity | 5 | 11 |
GO:0005267 | potassium channel activity | 6 | 11 |
GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 11 |
GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 11 |
GO:0015079 | potassium ion transmembrane transporter activity | 6 | 11 |
GO:0015267 | channel activity | 4 | 11 |
GO:0015269 | calcium-activated potassium channel activity | 7 | 11 |
GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 11 |
GO:0016286 | small conductance calcium-activated potassium channel activity | 8 | 11 |
GO:0022803 | passive transmembrane transporter activity | 3 | 11 |
GO:0022836 | gated channel activity | 5 | 11 |
GO:0022839 | monoatomic ion gated channel activity | 6 | 11 |
GO:0022857 | transmembrane transporter activity | 2 | 11 |
GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 11 |
GO:0046873 | metal ion transmembrane transporter activity | 5 | 11 |
GO:0005488 | binding | 1 | 1 |
GO:0005515 | protein binding | 2 | 1 |
GO:0005516 | calmodulin binding | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 287 | 291 | PF00656 | 0.355 |
CLV_NRD_NRD_1 | 379 | 381 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 410 | 412 | PF00675 | 0.359 |
CLV_NRD_NRD_1 | 478 | 480 | PF00675 | 0.467 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.401 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.366 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.467 |
CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.489 |
CLV_PCSK_PC1ET2_1 | 59 | 61 | PF00082 | 0.525 |
CLV_PCSK_SKI1_1 | 174 | 178 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 254 | 258 | PF00082 | 0.295 |
CLV_PCSK_SKI1_1 | 469 | 473 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 74 | 78 | PF00082 | 0.395 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.387 |
DEG_APCC_DBOX_1 | 412 | 420 | PF00400 | 0.456 |
DEG_APCC_DBOX_1 | 519 | 527 | PF00400 | 0.515 |
DEG_SPOP_SBC_1 | 246 | 250 | PF00917 | 0.535 |
DOC_CKS1_1 | 194 | 199 | PF01111 | 0.324 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.609 |
DOC_MAPK_gen_1 | 261 | 270 | PF00069 | 0.477 |
DOC_MAPK_gen_1 | 363 | 372 | PF00069 | 0.614 |
DOC_MAPK_gen_1 | 375 | 384 | PF00069 | 0.566 |
DOC_MAPK_gen_1 | 390 | 398 | PF00069 | 0.575 |
DOC_MAPK_gen_1 | 455 | 464 | PF00069 | 0.635 |
DOC_MAPK_gen_1 | 478 | 486 | PF00069 | 0.645 |
DOC_MAPK_HePTP_8 | 258 | 270 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 217 | 225 | PF00069 | 0.324 |
DOC_MAPK_MEF2A_6 | 261 | 270 | PF00069 | 0.539 |
DOC_MAPK_MEF2A_6 | 457 | 466 | PF00069 | 0.633 |
DOC_MAPK_RevD_3 | 396 | 411 | PF00069 | 0.435 |
DOC_PP1_RVXF_1 | 313 | 320 | PF00149 | 0.257 |
DOC_PP2B_LxvP_1 | 384 | 387 | PF13499 | 0.585 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 28 | 32 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 488 | 492 | PF00917 | 0.697 |
DOC_USP7_MATH_1 | 549 | 553 | PF00917 | 0.584 |
DOC_USP7_UBL2_3 | 89 | 93 | PF12436 | 0.706 |
DOC_WW_Pin1_4 | 176 | 181 | PF00397 | 0.318 |
DOC_WW_Pin1_4 | 193 | 198 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 305 | 310 | PF00397 | 0.243 |
DOC_WW_Pin1_4 | 50 | 55 | PF00397 | 0.576 |
LIG_14-3-3_CanoR_1 | 174 | 180 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 217 | 222 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 237 | 246 | PF00244 | 0.480 |
LIG_14-3-3_CanoR_1 | 263 | 269 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 282 | 287 | PF00244 | 0.157 |
LIG_14-3-3_CanoR_1 | 363 | 372 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 392 | 397 | PF00244 | 0.543 |
LIG_14-3-3_CanoR_1 | 532 | 540 | PF00244 | 0.602 |
LIG_Actin_WH2_2 | 98 | 115 | PF00022 | 0.517 |
LIG_BRCT_BRCA1_1 | 139 | 143 | PF00533 | 0.235 |
LIG_BRCT_BRCA1_1 | 178 | 182 | PF00533 | 0.360 |
LIG_BRCT_BRCA1_1 | 247 | 251 | PF00533 | 0.533 |
LIG_CaM_IQ_9 | 367 | 383 | PF13499 | 0.588 |
LIG_deltaCOP1_diTrp_1 | 290 | 296 | PF00928 | 0.243 |
LIG_EH1_1 | 183 | 191 | PF00400 | 0.360 |
LIG_EH1_1 | 346 | 354 | PF00400 | 0.563 |
LIG_EVH1_2 | 197 | 201 | PF00568 | 0.391 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.373 |
LIG_FHA_1 | 165 | 171 | PF00498 | 0.529 |
LIG_FHA_1 | 253 | 259 | PF00498 | 0.498 |
LIG_FHA_1 | 260 | 266 | PF00498 | 0.423 |
LIG_FHA_1 | 393 | 399 | PF00498 | 0.558 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.487 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.682 |
LIG_FHA_1 | 426 | 432 | PF00498 | 0.554 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.687 |
LIG_FHA_1 | 76 | 82 | PF00498 | 0.583 |
LIG_FHA_1 | 94 | 100 | PF00498 | 0.525 |
LIG_FHA_2 | 522 | 528 | PF00498 | 0.679 |
LIG_LIR_Gen_1 | 179 | 190 | PF02991 | 0.429 |
LIG_LIR_Gen_1 | 295 | 304 | PF02991 | 0.279 |
LIG_LIR_Gen_1 | 325 | 333 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 334 | 342 | PF02991 | 0.288 |
LIG_LIR_Gen_1 | 460 | 471 | PF02991 | 0.573 |
LIG_LIR_Gen_1 | 53 | 63 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 290 | 296 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 301 | 307 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 334 | 340 | PF02991 | 0.358 |
LIG_LIR_Nem_3 | 436 | 442 | PF02991 | 0.655 |
LIG_LIR_Nem_3 | 460 | 466 | PF02991 | 0.559 |
LIG_LIR_Nem_3 | 53 | 58 | PF02991 | 0.566 |
LIG_LIR_Nem_3 | 79 | 85 | PF02991 | 0.578 |
LIG_NRBOX | 205 | 211 | PF00104 | 0.260 |
LIG_PDZ_Class_1 | 551 | 556 | PF00595 | 0.659 |
LIG_Pex14_1 | 322 | 326 | PF04695 | 0.321 |
LIG_PTB_Apo_2 | 165 | 172 | PF02174 | 0.533 |
LIG_PTB_Apo_2 | 209 | 216 | PF02174 | 0.324 |
LIG_PTB_Apo_2 | 224 | 231 | PF02174 | 0.345 |
LIG_PTB_Phospho_1 | 224 | 230 | PF10480 | 0.374 |
LIG_REV1ctd_RIR_1 | 249 | 258 | PF16727 | 0.583 |
LIG_SH2_CRK | 219 | 223 | PF00017 | 0.324 |
LIG_SH2_CRK | 337 | 341 | PF00017 | 0.488 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.440 |
LIG_SH2_GRB2like | 224 | 227 | PF00017 | 0.425 |
LIG_SH2_PTP2 | 82 | 85 | PF00017 | 0.607 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.324 |
LIG_SH2_STAP1 | 394 | 398 | PF00017 | 0.596 |
LIG_SH2_STAT5 | 175 | 178 | PF00017 | 0.499 |
LIG_SH2_STAT5 | 224 | 227 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.600 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.349 |
LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.635 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.586 |
LIG_SH2_STAT5 | 463 | 466 | PF00017 | 0.604 |
LIG_SH2_STAT5 | 82 | 85 | PF00017 | 0.589 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.676 |
LIG_Sin3_3 | 149 | 156 | PF02671 | 0.196 |
LIG_SUMO_SIM_anti_2 | 482 | 488 | PF11976 | 0.660 |
LIG_SUMO_SIM_anti_2 | 98 | 103 | PF11976 | 0.533 |
LIG_SUMO_SIM_par_1 | 124 | 130 | PF11976 | 0.402 |
LIG_SUMO_SIM_par_1 | 394 | 399 | PF11976 | 0.585 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.529 |
LIG_TYR_ITIM | 302 | 307 | PF00017 | 0.284 |
LIG_UBA3_1 | 150 | 155 | PF00899 | 0.324 |
LIG_WRC_WIRS_1 | 232 | 237 | PF05994 | 0.527 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.412 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.578 |
MOD_CK1_1 | 240 | 246 | PF00069 | 0.624 |
MOD_CK1_1 | 295 | 301 | PF00069 | 0.290 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.645 |
MOD_CK1_1 | 310 | 316 | PF00069 | 0.237 |
MOD_CK1_1 | 474 | 480 | PF00069 | 0.619 |
MOD_CK1_1 | 7 | 13 | PF00069 | 0.780 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.803 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.627 |
MOD_CK2_1 | 521 | 527 | PF00069 | 0.611 |
MOD_DYRK1A_RPxSP_1 | 29 | 33 | PF00069 | 0.627 |
MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.604 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.361 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.375 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.471 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.500 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.309 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.474 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.426 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.640 |
MOD_GSK3_1 | 331 | 338 | PF00069 | 0.214 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.559 |
MOD_GSK3_1 | 415 | 422 | PF00069 | 0.656 |
MOD_GSK3_1 | 425 | 432 | PF00069 | 0.649 |
MOD_GSK3_1 | 50 | 57 | PF00069 | 0.616 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.698 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.669 |
MOD_N-GLC_1 | 138 | 143 | PF02516 | 0.360 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.315 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.318 |
MOD_NEK2_1 | 143 | 148 | PF00069 | 0.329 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.518 |
MOD_NEK2_1 | 292 | 297 | PF00069 | 0.278 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.346 |
MOD_NEK2_1 | 358 | 363 | PF00069 | 0.600 |
MOD_NEK2_1 | 396 | 401 | PF00069 | 0.536 |
MOD_NEK2_1 | 423 | 428 | PF00069 | 0.629 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.432 |
MOD_NEK2_1 | 472 | 477 | PF00069 | 0.690 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.714 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.579 |
MOD_NEK2_2 | 54 | 59 | PF00069 | 0.568 |
MOD_PIKK_1 | 521 | 527 | PF00454 | 0.620 |
MOD_PK_1 | 217 | 223 | PF00069 | 0.412 |
MOD_PKA_1 | 409 | 415 | PF00069 | 0.537 |
MOD_PKA_2 | 28 | 34 | PF00069 | 0.767 |
MOD_PKA_2 | 4 | 10 | PF00069 | 0.654 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.575 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.589 |
MOD_Plk_1 | 138 | 144 | PF00069 | 0.287 |
MOD_Plk_4 | 124 | 130 | PF00069 | 0.331 |
MOD_Plk_4 | 138 | 144 | PF00069 | 0.273 |
MOD_Plk_4 | 217 | 223 | PF00069 | 0.383 |
MOD_Plk_4 | 247 | 253 | PF00069 | 0.558 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.229 |
MOD_Plk_4 | 322 | 328 | PF00069 | 0.378 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.370 |
MOD_Plk_4 | 392 | 398 | PF00069 | 0.546 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.540 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.654 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.628 |
MOD_Plk_4 | 480 | 486 | PF00069 | 0.636 |
MOD_ProDKin_1 | 176 | 182 | PF00069 | 0.318 |
MOD_ProDKin_1 | 193 | 199 | PF00069 | 0.412 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.709 |
MOD_ProDKin_1 | 305 | 311 | PF00069 | 0.243 |
MOD_ProDKin_1 | 50 | 56 | PF00069 | 0.575 |
MOD_SUMO_rev_2 | 422 | 428 | PF00179 | 0.487 |
TRG_DiLeu_BaEn_1 | 354 | 359 | PF01217 | 0.434 |
TRG_DiLeu_BaLyEn_6 | 64 | 69 | PF01217 | 0.619 |
TRG_ENDOCYTIC_2 | 219 | 222 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 232 | 235 | PF00928 | 0.634 |
TRG_ENDOCYTIC_2 | 304 | 307 | PF00928 | 0.284 |
TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.299 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.423 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.448 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.590 |
TRG_ENDOCYTIC_2 | 463 | 466 | PF00928 | 0.604 |
TRG_ENDOCYTIC_2 | 82 | 85 | PF00928 | 0.578 |
TRG_ER_diArg_1 | 362 | 365 | PF00400 | 0.589 |
TRG_ER_diArg_1 | 409 | 411 | PF00400 | 0.554 |
TRG_NLS_MonoExtN_4 | 378 | 384 | PF00514 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 421 | 425 | PF00026 | 0.461 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P4A8 | Leptomonas seymouri | 67% | 100% |
A0A0S4IWT9 | Bodo saltans | 35% | 100% |
A0A1X0NNP7 | Trypanosomatidae | 44% | 100% |
A0A3S7WSZ6 | Leishmania donovani | 80% | 100% |
A0A422NNK5 | Trypanosoma rangeli | 42% | 100% |
A4HVZ6 | Leishmania infantum | 80% | 100% |
E9APP8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 77% | 100% |
Q4QFT1 | Leishmania major | 79% | 100% |
V5BNC5 | Trypanosoma cruzi | 41% | 100% |